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EP0475127B1 - Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher Temperatur - Google Patents

Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher Temperatur Download PDF

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Publication number
EP0475127B1
EP0475127B1 EP91113855A EP91113855A EP0475127B1 EP 0475127 B1 EP0475127 B1 EP 0475127B1 EP 91113855 A EP91113855 A EP 91113855A EP 91113855 A EP91113855 A EP 91113855A EP 0475127 B1 EP0475127 B1 EP 0475127B1
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Prior art keywords
group
carbon atoms
polyacetal resin
weight
resin composition
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French (fr)
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EP0475127A1 (de
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Hiroshi Tsukahara
Masahiko Niino
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Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
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Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4054—Mixtures of compounds of group C08G18/60 with other macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/205—Compounds containing groups, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
    • C08K5/31—Guanidine; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
    • C08L59/02—Polyacetals containing polyoxymethylene sequences only
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers

Definitions

  • the present invention relates to a novel polyacetal resin composition, and more particularly to a polyacetal resin composition simultaneously having an excellent high-temperature stiffness and an excellent lubricity.
  • Polyacetal resin is an engineering resin excellent in strength characteristics, fatigue resistance, self-lubricating property, etc., and is extensively in use in many fields such as automobiles, machines, electrical industry, electronic industry and the like.
  • polyamide resin is an engineering resin excellent in impact resistance, frictional resistance, abrasion resistance, flexibility, etc., and is extensively in use in many fields such as automobiles, machines, electrical industry, electronic industry and the like, similarly to polyacetal resin.
  • polymer alloys such as a polymer alloy formed between polyacetal resin and polyolefin resin are observed with interest.
  • a polyacetal resin composition prepared by adding 1-40 parts by weight of an inorganic powdery material to 100 parts by weight of a composition consisting of 5% by volume or more of a polyacetal resin and 95% by volume or less of a polyamide resin (Japanese Patent Application Kokai (Laid-Open) No. 63-34377) and a polyacetal resin composition prepared by dispersing a polyamide having a maximum particle diameter of 10 ⁇ m and consisting of 90% by weight or more of a polyacetal resin and 0.01-10% by weight of a polyamide resin (4,6-nylon) into a polyacetal resin (Japanese Patent Publication No.
  • a polymer alloy comprising a polyacetal resin, a polyamide resin, a dispersant and a filler which is excellent in high-temperature stiffness and lubricity, and has a good color tone.
  • composition according to the present invention remarkably improves the reinforcing effect and lubricity which have been problems of the above-mentioned prior art.
  • the present invention relates to a polyacetal resin composition
  • a polyacetal resin composition comprising 0.05-20 parts by weight of a dispersant (B) and 5-40 parts by weight of a filler (C), and 100 parts by weight of a resin ingredient (A) which comprises 90-50% by weight of a polyacetal resin (a) and 10-50% by weight of a polyamide resin (b) having a melting point of up to 230°C, a maximum particle diameter of 0.03-10 ⁇ m, determined by observing a 10 nm thick specimen of the polyacetal composition containing no filler (C) by means of a transmission electron microscope, and a maximum aspect ratio of up to 2, said polyamide resin being dispersed in a matrix of said polyacetal resin (a), wherein said filler (C) is at least one member selected from the group consisting of potassium titanate whisker, carbon whisker, glass fiber, carbon fiber, and organic fiber, and wherein said dispersant (B) is at least one member selected from the group consisting of a
  • Figures 1(a) and 1(b) are each a scanning electron microscopic photograph illustrating a rupture cross-section of one example of molded product made of a composition of the present invention.
  • Figures 2(a) and 2(b) are each a scanning electron microscopic photograph illustrating a rupture cross-section of one example of a molded product made of a composition of the present invention, but which contained no polyamide resin.
  • Figures 3(a) and 3(b) are each a transmission type electron microscopic photograph illustrating the morphology of one example of a composition of the present invention, but which contained no filler.
  • Figures 4(a) and 4(b) are each a transmission type electron microscopic photograph illustrating the morphology of one example of a composition of the present invention, but which contained no dispersant and no filler.
  • the polyacetal resin used in the present invention may be any oxymethylene homopolymer or copolymer.
  • the oxymethylene homopolymer is obtained by polymerizing formaldehyde or any of its cyclic oligomers such as trimer (trioxane), tetramer (tetraoxane) and the like, and is constituted substantially of oxymethylene units ⁇ CH2O ⁇ .
  • the oxymethylene copolymer is comprised of a polymeric structure in which oxyalkylene units other than oxymethylene are randomly introduced into a chain constituted of oxymethylene units.
  • the content of said other oxyalkylene units in the oxymethylene copolymer is preferably selected from a range of 0.05-50 moles and more preferably from a range of 0.1-20 moles, both being per 100 moles of the oxymethylene unit.
  • an oxyethylene unit, straight or branched chain oxypropylene unit, straight or branched chain oxybutylene unit, oxyphenylene unit and the like can be referred to.
  • the introduction of one or more types of oxyalkylene units are allowable.
  • the oxyethylene unit ⁇ (CH2)2O ⁇ and the straight chain oxybutylene unit (oxytetramethylene unit) ⁇ (CH2)4O ⁇ are particularly preferable from the viewpoint of improving the physical properties of the polyacetal resin composition.
  • the oxymethylene copolymers are obtained by copolymerizing formaldehyde or a cyclic oligomer of formaldehyde such as trioxane, tetraoxane and the like, with a cyclic ether such as ethylene oxide, propylene oxide, epichlorohydrin, 1,3-dioxolane, glycol formal, diglycol formal and the like.
  • Oxymethylene block copolymers wherein at least 50% by mole of the main chain is constituted of oxymethylene units and the remainder is constituted of units other than oxymethylene are also included in the oxymethylene copolymer referred to in the present invention.
  • composition of the present invention one type of said polyacetal resin or two or more types in combination may be used.
  • nylons such as nylon 11, nylon 12, nylon 6, nylon 610, nylon 12 and copolymers of these nylons, polyamide resins containing in its molecular chain 0.1-50% by weight of straight chain alkylene oxide units having 1-10 carbon atoms, polyamide resins containing in its molecular chain 0.1-50% by weight of straight chain alkyl ester units having 1-10 carbon atoms, polyamide resins wherein the amide bond hydrogen of the main chain is partially substituted by an alkoxymethyl group such as a methoxymethyl group, copolymers of these polyamides, and the like can be referred to.
  • these polyamide resins those having a melting point of up to 230°C are used in the present invention. In the present invention, one type of these polyamide resins or two or more types in combination may be used.
  • the polyacetal resin and the polyamide resin in a ratio, such that 90-50% by weight of polyacetal resin and 10-50% by weight of polyamide resin, preferably 90-60% by weight of polyacetal resin and 10-40% by weight of polyamide resin, and more preferably 90-70% by weight of polyacetal resin and 10-30% by weight of polyamide resin are used based on the total weight of the resin ingredient.
  • the amount of polyacetal resin is smaller than 50% by weight, the composition obtained therefrom cannot sufficiently exhibit the characteristic properties of polyacetal resin and therefore the object of the present invention cannot be achieved. If the amount of polyacetal resin exceeds 90% by weight, the characteristic properties of polyamide resin cannot sufficiently be exhibited, and therefore the object of the present invention cannot be achieved.
  • melamine derivatives represented by the following general formula (I): wherein R1 to R6 each represents a hydrogen atom, a straight or branched chain alkyl group having 1-30 carbon atoms, a cycloalkyl group having 3-30 carbon atoms, an aryl group or -(CH2) m -OR7 (R7 represents a straight chain alkyl group having 1-5 carbon atoms and m represents an integer of 1-4), wherein at least one of R1 to R4 is -(CH2) m -OR7; urea derivatives represented by the following general formula (II): wherein R8 to R11 each represents a hydrogen atom, a straight or branched chain alkyl group having 1-30 carbon atoms, a cycloalkyl group having 3-30 carbon atoms, an aryl group or -(CH2) n -OR1 (R1 represents a straight chain alkyl group
  • Examples of the melamine derivatives represented by general formula (I) include the following compounds such as monomethoxymethylmelamine, dimethoxymethylmelamine, trimethoxymethylmelamine, tetramethoxymethylmelamine, pentamethoxymethylmelamine, hexamethoxymethylmelamine, and derivatives of these compounds obtained by partially or wholly replacing the methoxy groups of these compounds with at least one member selected from the group consisting of ethoxy group, n-propoxy group, iso-propoxy group, n-butoxy group, iso-butoxy group, sec-butoxy group, t-butoxy group, pentyloxy group and the like.
  • Examples of the urea derivative represented by general formula (II) include the following compounds such as N-methoxymethylurea, N,N-dimethoxymethylurea, N-N'-dimethoxymethylurea, N-methoxymethyl-N'-methylurea, N,N-dimethoxymethyl-N',N'-dimethylurea, N,N,N'-trimethoxy-methylurea, N,N-dimethoxymethyl-N'-ethylurea, and derivatives of these compounds obtained by partially or wholly replacing the methoxy groups of these compounds with at least one member selected from the group consisting of ethoxy group, n-propoxy group, iso-propoxy group, n-butoxy group, iso-butoxy group, sec-butoxy group, t-butoxy group, pentyloxy group and the like, etc.
  • aminoformic acid derivatives represented by general formula (III) include the following compounds such as N,N-dimethoxymethylaminoformic acid, N-methoxymethylaminoformic acid, methyl N-methoxymethylaminoformate, ethyl N-methoxymethylaminoformate, and derivatives of these compounds obtained by partially or wholly replacing the methoxy group of these compounds with at least one member selected from the group consisting of ethoxy group, n-propoxy group, iso-propoxy group, n-butoxy group, iso-butoxy group, sec-butoxy group, t-butoxy group, pentyloxy group and the like, etc.
  • Examples of the guanidine derivatives represented by general formula (IV) include the following compounds such as monomethoxymethylguanidine, dimethoxymethylguanidine, trimethoxymethylguanidine, tetramethoxymethylguanidine, and derivatives of these compounds obtained by partially or wholly replacing the methoxy groups of these compounds with at least one member selected from the group consisting of ethoxy group, n-propoxy group, iso-propoxy group, n-butoxy group, iso-butoxy group, sec-butoxy group, t-butoxy group, pentyloxy group and the like, etc.
  • the alkylene group in N-alkylalkoxy group has 1-4 carbon atoms, preferably 1 or 2 carbon atoms, and particularly preferably one carbon atom.
  • HMDI hexamethylene diisocyanate
  • MDI dicyclohexylmethane diisocyanate
  • MDI diphenylmethane diisocyanate
  • TDI tolylene diisocyanate
  • compounds obtained by releasing of CO2 from these compounds to a carbodiimide compounds obtained by modifying these compounds with an alcohol
  • isocyanates compounds of oligomers such as dimer, trimer, tetramer and the like, and all of the compounds having two or more functional groups reactive with alcoholic hydroxyl group such as compounds having two or more maleic anhydride units in one molecule are also included.
  • hexaalkoxymethylmelamine, tetraalkoxymethylurea, methyl N-alkoxymethylaminoformate and tetraalkoxyguanidine are preferable, and hexamethoxymethylmelamine, tetramethoxymethylurea, methyl N-methoxymethylaminoformate and tetramethoxymethylguanidine are particularly preferable.
  • one type of said dispersant or two or more types in combination may be used.
  • the amount of the dispersant is selected from a range of 0.05-20 parts by weight, preferably 0.1-10 parts by weight and more preferably 0.2-5 parts by weight, per 100 parts by weight of the sum of polyacetal resin (a) and polyamide resin (b). If this amount is less than 0.05 part by weight, a sufficient lubricity of the composition cannot be attained since the polyamide resin will not diffuse as a granular present in the matrix of the polyacetal resin. If the amount exceeds 20 parts by weight, heat stability of the composition would become greatly deteriorated, making the work of melting and kneading the composition to be difficult.
  • Fig. 4(A) magnification: 1,000 times
  • Fig. 4(B) magnification: 5,000 times
  • a super-thin specimen having a thickness of 100 nm was prepared from a composition of Comparative Example 1, which contains no glass fibers.
  • a polyamide resin is observed to form streaks in a polyacetal resin matrix.
  • glass fiber is more preferable.
  • the fiber length of the glass fiber is 0.1-10 mm, preferably 0.3-8.0 mm, and more preferably 0.5-7.0 mm. Its fiber diameter is 0.1-50 ⁇ m, preferably 5-20 ⁇ m, and more preferably 6-15 ⁇ m.
  • the glass fiber may be made of any of E glass and A glass, the glass fiber made of E glass is more preferable.
  • the glass fiber may have an untreated surface, or it may also be used after a surface treatment using various surface-treating agents.
  • silane couplers such as alkoxysilane, silazane, chlorosilane, aminosilane, glycidosilane and the like, titanate type couplers, aluminum type couplers, urethane type treating agents and the like can be referred to.
  • aminosilane is particularly preferable.
  • the surface treatment exhibits its effect not only on glass fiber but also on other fillers.
  • one type of filler or two or more types in combination may be used.
  • the amount of said filler (C) is selected from a range of 5-40 parts by weight, preferably 7-35 parts by weight and more preferably 10-30 parts by weight, per 100 parts by weight of the sum of polyacetal resin (a) and polyamide resin (b). If this amount is smaller than 5 parts by weight, the effect of improving high-temperature stiffness and lubricity cannot be exhibited sufficiently. If the amount exceeds 40 parts by weight, heat stability would become greatly deteriorated, making the work of melting and kneading the composition to be difficult.
  • the polyamide resin in the polyacetal resin composition of the present invention, it is desirable to prepare the polyamide resin in a manner, such that it is present in a particle form having a maximum particle diameter of 0.03-10 ⁇ m, preferably 0.05-8 ⁇ m, and a maximum aspect ratio of 2 or less, preferably 1.8 or less, when the resin composition contains no filler (C).
  • maximum particle diameter means the longest particle diameter of polyamide resin particles existing in polyacetal resin medium which can be observed by preparing a super-thin specimen having a thickness of 10 nm from a polyacetal resin composition of the present invention containing no filler (C) and observing its morphology by means of a transmission type electron microscope. In other words, it means such a large size present that no other size present which exceeds it can be found in any other specimens.
  • FIG. 3(A) magnification: 1,000 times
  • Fig. 3(B) magnification: 5,000 times
  • Figs. 3(A) and 3(B) are electron transmission microphotographs of a super-thin specimen having a thickness of 100 nm prepared from the composition of Example 2 minutely described below, from which fillers were excluded so as to enable one to easily observe the morphology of the resin.
  • maximum aspect ratio means the maximum value of (maximum particle diameter)/(minimum particle diameter) ratio of the polyamide resin present.
  • additive components which are conventionally added to thermoplastic resins.
  • additives include antioxidant, heat stabilizer, plasticizer, ultraviolet absorber, lubricant, flame retardant, pigment and the like.
  • thermoplastic resin composition of the present invention is not critical, but methods having been conventionally adopted in the preparation of thermoplastic resin compositions up to the present time can be used.
  • it can be prepared, by melting and kneading the above-mentioned ingredients (a), (b), (B), (C) and optionally used additive components, by the use of known apparatuses conventionally used for kneading molten resins, such as Bunbury mixer, roll kneader, extruder, ball mill, high-speed agitater, shaker and the like.
  • the extruder is most desirable from the viewpoint of interruption of oxygen, working environment, working efficiency, etc.
  • the types of extruders single shaft type, double shaft type, vent type, no-vent type, etc. can be referred to. With any of these extruders, the composition of the present invention can be prepared.
  • the conditions of extrusion are not critical, so far as the conditions are those which are conventionally adopted in the preparation of thermoplastic resin compositions.
  • the maximum resin temperature is 210°C or above, more preferably 220°C or above, and the time period of melting and kneading is 0.2 minute or longer, more preferably 0.5 minute or longer. If the maximum resin temperature is lower than 210°C or the time period of melting and kneading is shorter than 0.2 minute, it is difficult to obtain a composition having the intended high-temperature stiffness and lubricity.
  • the term "maximum resin temperature” means the equilibrium resin temperature under predetermined conditions of melting and kneading which can be detected by a thermometer provided in the system, when the melting-kneading machine is a batchwise kneading machine such as kneader, roll mill and the like.
  • the term “maximum resin temperature” means an equilibrium temperature of a resin just after being extruded out of the extruder under predetermined conditions of melting and kneading.
  • time period of melting and kneading means a period of time measured from the time when resin temperature has reached the above-mentioned maximum resin temperature. Particularly when the melting-kneading machine is an extruder, it indicates a mean residence time in a state where a resin has reached the maximum resin temperature.
  • the mean residence time is the period from a time when a black-colored pigment (acetylene black) is added through the raw material feeding hole in an amount of 5% by weight to a time when the resin discharged from die has become assuming the deepest color.
  • the polyacetal resin composition of the present invention can be used as a material for sliding parts, precision parts and the like where a polyacetal resin is conventionally used and as a material for sliding parts, impact-resistant parts, composite parts and the like where a polyamide resin is conventionally used. More specifically, the resin composition of the present invention is successfully usable as an elementary material for gear, bearing, lever, key stem, cam, ratchet, roller, screw, water feeding parts, toy parts, fan, film, silksworm gut, pipe, filament, tube and precision composite materials reinforced with fillers.
  • test piece of flexural test was prepared by melting and kneading a composition and forming it by means of a forming machine in which the cylinder temperature had been adjusted to 200°C according to ASTM D-790 (die temperature 70°C, cooling time 20 seconds).
  • Average coefficient of friction was determined according to JIS K-7218.
  • a super-thin specimen having a thickness of 100 nm was prepared from a polyacetal resin composition of the present invention, but which contained no filler, and its morphology was examined by means of transmission type electron microscope.
  • the longest particle diameter of polyamide resin (b) present in the polyacetal resin (a) was taken as maximum particle diameter.
  • the ratio of maximum particle diameter of the polyamide resin present to its minimum particle diameter was taken as the maximum aspect ratio.
  • the morphology could also be examined similarly by observing the rupture cross-section of a resin ingredient (A) containing filler with scanning electron microscope (SEM).
  • Resin compositions were prepared by melting, kneading and pelletizing polyacetal resin (a), polyamide resin (b), dispersant (B) and filler (C) of which types and amounts were as shown in Table 1.
  • Resin compositions were prepared by melting, kneading and pelletizing polyacetal resin (a), polyamide resin (b), dispersant (B) and filler (C) of which types and amounts were as shown in Table 2.
  • Figs. 1(A) and 1(B) illustrate the rupture cross-section of a molded product of the composition of Example 2 of the present invention
  • Figs. 2(A) and 2(B) illustrate the rupture cross-section of a molded product of the composition of Comparative Example 6.
  • thermoplastic resin composition of the present invention is a polyacetal resin composition comprising a polyacetal resin, a polyamide resin, a dispersant and a filler. Unlike prior polyacetal resin compositions, it simultaneously has excellent high-temperature stiffness and lubricity and has a good color tone.

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Claims (12)

  1. Polyacetal-Harzzusammensetzung, enthaltend 0,05 bis 20 Gew.-Teile eines Dispergiermittels (B) und 5 bis 40 Gew.-Teile eines Füllstoffes (C) und 100 Gew.-Teile eines Harzbestandteils (A), der 90 bis 50 Gew.-% eines Polyacetalharzes (a) und 10 bis 50 Gew.-% eines Polyamidharzes (b) umfaßt, das einen Schmelzpunkt bis zu 230°C, einen maximalen Teilchendurchmesser von 0,03 bis 10 µm, bestimmt durch Betrachtung einer 10 nm dicken Probe der keinen Füllstoff (C) enthaltenden Polyacetalzusammensetzung mit Hilfe eines Transmissions-Elektronenmikroskops, und ein maximales Länge-Dicke-Verhältnis bis zu 2 aufweist, wobei das Polyamidharz in einer Matrix des Polyacetalharzes (a) dispergiert ist,
    wobei der Füllstoff (C) mindestens ein aus der aus Kaliumtitanat-Whisker, Kohlenstoff-Whisker, Glasfaser, Kohlenstoffaser und organischen Fasern bestehenden Gruppe ausgewähltes Mitglied ist und wobei das Dispergiermittel (B) mindestens ein Mitglied ist, das aus der Gruppe der folgenden Verbindungen ausgewählt ist:
    Melaminderivaten der folgenden allgemeinen Formel (I):
    Figure imgb0019
     worin R¹ bis R⁶ jeweils ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen, eine Arylgruppe oder -(CH₂)m-OR⁷ bedeuten (R⁷ bedeutet eine geradekettige Alkylgruppe mit 1 bis 5 Kohlenstoffatomen und m bedeutet eine ganze Zahl von 1 bis 4), wobei mindestens eines von R¹ bis R⁴ -(CH₂)m-OR⁷ ist, Harnstoffderivaten der folgenden allgemeinen Formel (II):
    Figure imgb0020
     worin R⁸ bis R¹¹ jeweils ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen, eine Arylgruppe oder -(CH₂)n-OR¹ bedeuten (R¹ bedeutet eine geradekettige Alkylgruppe mit 1 bis 5 Kohlenstoffatomen und n bedeutet eine ganze Zahl von 1 bis 4), wobei mindestens eines von R⁸ bis R¹¹ -(CH₂)n-OR¹ ist, Aminoameisensäurederivaten der folgenden allgemeinen Formel (III):
    Figure imgb0021
     worin R¹³ und R¹⁴ jeweils ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen, eine Arylgruppe oder -(CH₂)p-OR¹⁶ bedeuten (R¹⁶ bedeutet eine geradekettige Alkylgruppe mit 1 bis 5 Kohlenstoffatomen und p bedeutet eine ganze Zahl von 1 bis 4), wobei mindestens eines von R¹³ und R¹⁴ -(CH₂)p-OR¹⁶ ist, und R¹⁵ ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen oder eine Arylgruppe bedeutet, und
    Guanidinderivaten der folgenden allgemeinen Formel (IV):
    Figure imgb0022
     worin R¹⁷ bis R⁰ jeweils ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen, eine Arylgruppe oder -(CH₂)q-OR bedeuten (R bedeutet eine geradekettige Alkylgruppe mit 1 bis 5 Kohlenstoffatomen und q bedeutet eine ganze Zahl von 1 bis 4), wobei mindestens eines von R¹⁷ bis R⁰ -(CH₂)q-OR ist, und R¹ ein Wasserstoffatom, eine geradekettige oder verzweigtkettige Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine Cycloalkylgruppe mit 3 bis 30 Kohlenstoffatomen oder eine Arylgruppe bedeutet,
    oder ausgewählt ist unter (V) Hexamethylendiisocyanat (HMDI), Dicyclohexylmethandiisocyanat, Isophorondiisocyanat, Diphenylmethandiisocyanat (MDI), Phenylendiisocyanat oder Tolylendiisocyanat (TDI), oder
    wobei das Dispergiermittel (B) (VI) eine Carbodiimidverbindung ist, die durch Modifizieren eines aus der aus Hexamethylendiisocyanat (HMDI), Dicyclohexylmethandiisocyanat, Isophorondiisocyanat, Diphenylmethandiisocyanat (MDI), Phenylendiisocyanat oder Tolylendiisocyanat (TDI) bestehenden Gruppe ausgewählten Mitglieds mit einem Alkohol, einem Isocyanat-Oligomeren oder einer Verbindung mit zwei oder mehr funktionellen Gruppen, die gegenüber alkoholischen Hydoxylgruppen reaktiv sind, erhalten wird.
  2. Polyacetal-Harzzusammensetzung nach Anspruch 1, wobei das Polyamidharz (b) mindestens ein Mitglied, ausgewählt aus der Gruppe ist, die aus einem Nylon, einem Polyamidharz, in dessen Molekülkette 0,1 bis 50 Gew.-%, bezogen auf die Kette, Alkylenoxideinheiten mit 1 bis 10 Kohlenstoffatomen enthalten sind, einem Polyamidharz, in dessen Molekülkette 0,1 bis 50 Gew.-%, bezogen auf die Kette, Alkylestereinheiten mit 1 bis 10 Kohlenstoffatomen enthalten sind, und einem Polyamidharz, in dem Wasserstoff in der Amidbindung der Hauptkette teilweise durch eine Alkoxymethylgruppe ersetzt ist, besteht.
  3. Polyacetal-Harzzusammensetzung nach Anspruch 2, wobei das Nylon aus der aus Nylon-11, Nylon-12, Nylon-6, Nylon-610 und Nylon-612 bestehenden Gruppe ausgewählt ist.
  4. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 3, wobei die Alkoxymethylgruppe eine Methoxymethylgruppe ist.
  5. Polyacetal-Harzzusammensetzung nach Anspruch 2 oder 4, wobei das Polyamidharz (b) ein Copolymer ist.
  6. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 5, wobei die Verbindung, die zwei oder mehr gegenüber alkoholischen Hydroxylgruppen reaktive funktionelle Gruppen aufweist, die zur Herstellung der Carbodiimidverbindung VI verwendet wird, eine Verbindung ist, die in einem Molekül zwei oder mehr Anhydrideinheiten enthält.
  7. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 6, wobei der Harzbestandteil (A) 90 bis 60 Gew.-% des Polyacetalharzes (a) und 10 bis 40 Gew.-% des Polyamidharzes (b) enthält.
  8. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 7, die 0,1 bis 10 Gew.-Teile des Dispergiermittels (B) enthält.
  9. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 8, die 7 bis 35 Gew.-Teile des Füllstoffes (C) enthält.
  10. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 9, wobei das Dispergiermittel (B) mindestens ein Mitglied ist, das aus der aus einem Hexaalkoxymethylmelamin, einem Tetraalkoxymethylharnstoff, einem Methyl-N-alkoxy-methylaminoformiat und einem Tetraalkoxyguanidin bestehenden Gruppe ausgewählt ist.
  11. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 10, wobei der Füllstoff (C) mit dem Polyamidharz (b) beschichtet ist.
  12. Polyacetal-Harzzusammensetzung nach einem der Ansprüche 1 bis 11, wobei der Füllstoff Glasfaser mit einer Länge von 0,3 bis 8,0 mm und einem Durchmesser von 0,1 bis 50 µm ist.
EP91113855A 1990-08-20 1991-08-19 Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher Temperatur Expired - Lifetime EP0475127B1 (de)

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JP3285480B2 (ja) * 1995-09-29 2002-05-27 ポリプラスチックス株式会社 ポリアセタール樹脂組成物
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US7067186B2 (en) * 2001-12-21 2006-06-27 Mitsubishi Gas Chemical Company, Inc. Thermoplastic resin composition
DE10297570B4 (de) * 2001-12-25 2008-02-21 Asahi Kasei Chemicals Corporation Verwendung einer Harzzusammensetzung mit Polyoxymethylenharz als Rampe
US6974849B2 (en) * 2003-03-03 2005-12-13 Ticona Llc Polyacetals with improved resistance to bleach
US8128845B2 (en) 2006-11-22 2012-03-06 E.I. Du Pont De Nemours And Company Static dissipative polyacetal compositions
WO2014126626A1 (en) 2013-02-15 2014-08-21 Empire Technology Development Llc Phenolic epoxy compounds
EP3008125A4 (de) 2013-06-13 2016-12-07 Empire Technology Dev Llc Multifunktionale phenolharze
WO2015084299A1 (en) * 2013-12-02 2015-06-11 Empire Technology Development Llc Gemini surfactants and methods for their preparation and use
WO2015084304A1 (en) 2013-12-02 2015-06-11 Empire Technology Development Llc Novel gemini surfactants and their use
US9896637B2 (en) * 2015-04-08 2018-02-20 Jtekt Corporation Sliding member, method of manufacturing sliding member, and gear
JP2017061638A (ja) * 2015-09-25 2017-03-30 富士ゼロックス株式会社 樹脂組成物、樹脂成形体、及び樹脂組成物の製造方法
WO2017064778A1 (ja) * 2015-10-14 2017-04-20 Ykk株式会社 ポリアセタール樹脂組成物、ファスニング部材及びスライドファスナー
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DE69117840T2 (de) 1996-11-07
FR2665904B1 (fr) 1993-12-31
JPH05239313A (ja) 1993-09-17
EP0475127A1 (de) 1992-03-18
GB2247684B (en) 1993-10-06
KR920004498A (ko) 1992-03-27
TW200514B (de) 1993-02-21
BE1004773A0 (fr) 1993-01-26
BE1004773B3 (fr) 1994-11-03
DE69117840D1 (de) 1996-04-18
GB2247684A (en) 1992-03-11
US5354798A (en) 1994-10-11
FR2665904A1 (fr) 1992-02-21
GB9117870D0 (en) 1991-10-09
KR950006140B1 (ko) 1995-06-09
JP3109753B2 (ja) 2000-11-20

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